EP3124450B1 - Sonnenschutzbeschichtungen mit unterbrochener metallschicht - Google Patents

Sonnenschutzbeschichtungen mit unterbrochener metallschicht Download PDF

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Publication number
EP3124450B1
EP3124450B1 EP16189418.3A EP16189418A EP3124450B1 EP 3124450 B1 EP3124450 B1 EP 3124450B1 EP 16189418 A EP16189418 A EP 16189418A EP 3124450 B1 EP3124450 B1 EP 3124450B1
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EP
European Patent Office
Prior art keywords
layer
coating
dielectric layer
article according
zinc
Prior art date
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Application number
EP16189418.3A
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English (en)
French (fr)
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EP3124450A1 (de
Inventor
Paul A. Medwick
Adam D. Polcyn
James P. Thiel
Andreas V. WAGNER
Harry Buhay
James J. Finley
Dennis J. O'shaughnessy
Abhinav Bhandari
Paul R. Ohodnicki, Jr.
Jeffrey A. Benigni
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Vitro Flat Glass LLC
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Vitro Flat Glass LLC
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Priority to EP20188402.0A priority Critical patent/EP3750855A1/de
Publication of EP3124450A1 publication Critical patent/EP3124450A1/de
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
    • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
    • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
    • C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
    • C03C17/3618—Coatings of type glass/inorganic compound/other inorganic layers, at least one layer being metallic
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
    • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
    • C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
    • C03C17/3639—Multilayers containing at least two functional metal layers
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
    • C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
    • C03C17/3602—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer
    • C03C17/3657—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal the metal being present as a layer the multilayer coating having optical properties
    • C03C17/366—Low-emissivity or solar control coatings
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00—Coatings on glass
    • C03C2217/40—Coatings comprising at least one inhomogeneous layer
    • C03C2217/42—Coatings comprising at least one inhomogeneous layer consisting of particles only
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/12—All metal or with adjacent metals
    • Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12535—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.] with additional, spatially distinct nonmetal component
    • Y10T428/12542—More than one such component
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/12—All metal or with adjacent metals
    • Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12535—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.] with additional, spatially distinct nonmetal component
    • Y10T428/12542—More than one such component
    • Y10T428/12549—Adjacent to each other
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
    • Y10T428/24851—Intermediate layer is discontinuous or differential
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
    • Y10T428/24917—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including metal layer

Definitions

  • This invention relates generally to solar control coatings and, in one particular embodiment, to a solar control coating having increased absorbance and asymmetrical reflectance.
  • Solar control coatings are known in the fields of architectural and automotive transparencies. These solar control coatings block or filter selected ranges of electromagnetic radiation, such as in the range of solar infrared or solar ultraviolet radiation, to reduce the amount of solar energy entering the vehicle or building. This reduction of solar energy transmittance helps reduce the load on the cooling units of the vehicle or building.
  • the transparency such as a windshield
  • the visible light transmittance can be lower.
  • US 2004/146645 A1 relates to an article having a sealed layered edge, e.g. an automotive laminate and a multiple glazed unit including a pair of glass sheet in a fixed relationship with one another.
  • a sputtered coating is deposited on a major surface of one of the sheets and includes at least one combination of a metal film, e.g. a silver film and a dielectric film.
  • Discontinuities in the metal film at the marginal edges of the coated sheet provide voids in the metal film to impede or stop corrosion of the metal film.
  • the discontinuities include break lines or segments in the coating, coating thickness variations provided by abrading the coating and spaced discrete coating areas on the marginal edges of the coated sheet.
  • the discontinuities may be made in the metal film using a laser, an abrasive surface, a coating mask and/or coating deletion techniques.
  • WO 96/13379 discloses a solar control film having low visible light transmittance and low visible light reflectance comprised of two or more transparent substrates each bearing a thin, transparent, discontinuous, incoherent film of metal having low visible light reflectance and a degree of visible light blocking capacity, the substrates being so assembled and laminated into a composite that the visible light blocking capacities of the metal films are effectively combined to provide a composite having low visible light transmittance as well as low visible light reflectance.
  • JP 2001 353810 A describes a transparent substrate coated with metal thin films each having a thickness of 1-30 nm and transparent thin films each having a thickness of 10 - 150 nm which are alternately laminated to the surface of the transparent substrate to form a transparent laminar block. At least one of the metal thin films in the laminar block is not of a continuous film structure.
  • a heat strengthened glass substrate is coated with a solar control coating having an absorber material, such as a nickel-chromium alloy material (e.g., Inconel®), to absorb visible light to darken the window.
  • This transparency also includes a relatively thick, continuous, infrared reflective metal layer to reflect solar energy, such as solar infrared energy.
  • a problem with this known transparency is that the glass substrate must be cut to a desired shape and tempered before the coating is applied. If the coating is applied before the glass substrate is tempered, the resultant coating becomes hazy during the high temperature processings required for the tempering process. This haze is aesthetically undesirable.
  • the present invention relates to a coated article comprising a substrate and a coating over at least a portion of the substrate as defined in appended claim 1.
  • the coating of the invention includes one or more continuous, infrared reflective metal layers in combination with a subcritical (i.e., discontinuous) metal layer.
  • the discontinuous metal layer increases the visible light absorption of the coating and, in combination with dielectric layers of appropriate thickness, can also provide the coated article with asymmetrical reflectance.
  • a coating of the invention comprises a plurality of metallic layers alternating with a plurality of dielectric layers, with at least one of the metallic layers comprising a subcritical metallic layer having discontinuous metal regions.
  • the coated article comprises a substrate and a coating stack over at least a portion of the substrate.
  • the coating stack comprises a plurality of metallic layers and a plurality of dielectric layers, wherein at least one of the metallic layers comprises a subcritical metallic layer having discontinuous metallic regions.
  • each numerical value should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.
  • the terms “formed over”, “deposited over”, or “provided over” mean formed, deposited, or provided on but not necessarily in contact with the surface.
  • a coating layer "formed over" a substrate does not preclude the presence of one or more other coating layers or films of the same or different composition located between the formed coating layer and the substrate.
  • the terms “polymer” or “polymeric” include oligomers, homopolymers, copolymers, and terpolymers, e.g., polymers formed from two or more types of monomers or polymers.
  • the terms “visible region” or “visible light” refer to electromagnetic radiation having a wavelength in the range of 380 nm to 800 nm.
  • the terms “infrared region” or “infrared radiation” refer to electromagnetic radiation having a wavelength in the range of greater than 800 nm to 100,000 nm.
  • the terms “ultraviolet region” or “ultraviolet radiation” mean electromagnetic energy having a wavelength in the range of 300 nm to less than 380 nm.
  • the term “film” refers to a coating region of a desired or selected coating composition.
  • a “layer” can comprise one or more “films”, and a “coating” or “coating stack” can comprise one or more “layers”.
  • asymmetrical reflectivity means that the visible light reflectance of the coating from one side is different than that of the coating from the opposite side.
  • critical thickness means a thickness above which a coating material forms a continuous, uninterrupted layer and below which the coating material forms discontinuous regions or islands of the coating material rather than a continuous layer.
  • subcritical thickness means a thickness below the critical thickness such that the coating material forms isolated, non-connected regions of the coating material.
  • the term “islanded” means that the coating material is not a continuous layer but, rather, that the material is deposited to form isolated regions or islands.
  • an architectural transparency such as, but not limited to, an insulating glass unit (IGU).
  • architectural transparency refers to any transparency located on a building, such as, but not limited to, windows and sky lights.
  • the invention is not limited to use with such architectural transparencies but could be practiced with transparencies in any desired field, such as, but not limited to, laminated or non-laminated residential and/or commercial windows, insulating glass units, and/or transparencies for land, air, space, above water and underwater vehicles.
  • the transparency 10 can have any desired visible light, infrared radiation, or ultraviolet radiation transmission and/or reflection.
  • the transparency 10 can have a visible light transmission of any desired amount, e.g., greater than 0% up to 100%.
  • the exemplary transparency 10 of Fig. 1 is in the form of a conventional insulating glass unit and includes a first ply 12 with a first major surface 14 (No. 1 surface) and an opposed second major surface 16 (No. 2 surface).
  • the first major surface 14 faces the building exterior, i.e., is an outer major surface
  • the second major surface 16 faces the interior of the building.
  • the transparency 10 also includes a second ply 18 having an outer (first) major surface 20 (No. 3 surface) and an inner (second) major surface 22 (No. 4 surface) and spaced from the first ply 12. This numbering of the ply surfaces is in keeping with conventional practice in the fenestration art.
  • the first and second plies 12, 18 can be connected together in any suitable manner, such as by being adhesively bonded to a conventional spacer frame 24.
  • a gap or chamber 26 is formed between the two plies 12, 18.
  • the chamber 26 can be filled with a selected atmosphere, such as air, or a non-reactive gas such as argon or krypton gas.
  • a solar control coating 30 (or any of the other coatings described below) is formed over at least a portion of one of the plies 12, 18, such as, but not limited to, over at least a portion of the No. 2 surface 16 or at least a portion of the No. 3 surface 20. Although, the coating could also be on the No. 1 surface or the No. 4 surface, if desired. Examples of insulating glass units are found, for example, in U.S. Patent Nos. 4,193,236 ; 4,464,874 ; 5,088,258 ; and 5,106,663 .
  • the plies 12, 18 of the transparency 10 can be of the same or different materials.
  • the plies 12, 18 can include any desired material having any desired characteristics.
  • one or more of the plies 12, 18 can be transparent or translucent to visible light.
  • transparent is meant having visible light transmission of greater than 0% up to 100%.
  • one or more of the plies 12, 18 can be translucent.
  • translucent is meant allowing electromagnetic energy (e.g., visible light) to pass through but diffusing this energy such that objects on the side opposite the viewer are not clearly visible.
  • suitable materials include, but are not limited to, plastic substrates (such as acrylic polymers, such as polyacrylates; polyalkylmethacrylates, such as polymethylmethacrylates, polyethylmethacrylates, polypropylmethacrylates, and the like; polyurethanes; polycarbonates; polyalkylterephthalates, such as polyethyleneterephthalate (PET), polypropyleneterephthalates, polybutyleneterephthalates, and the like; polysiloxane-containing polymers; or copolymers of any monomers for preparing these, or any mixtures thereof); ceramic substrates; glass substrates; or mixtures or combinations of any of the above.
  • plastic substrates such as acrylic polymers, such as polyacrylates; polyalkylmethacrylates, such as polymethylmethacrylates, polyethylmethacrylates, polypropylmethacrylates, and the like; polyurethanes; polycarbonates; polyalkylterephthalates, such as polyethyleneterephthal
  • one or more of the plies 12, 18 can include conventional soda-lime-silicate glass, borosilicate glass, or leaded glass.
  • the glass can be clear glass.
  • clear glass is meant non-tinted or non-colored glass.
  • the glass can be tinted or otherwise colored glass.
  • the glass can be annealed or heat-treated glass.
  • heat treated means tempered or at least partially tempered.
  • the glass can be of any type, such as conventional float glass, and can be of any composition having any optical properties, e.g., any value of visible transmission, ultraviolet transmission, infrared transmission, and/or total solar energy transmission.
  • float glass glass formed by a conventional float process in which molten glass is deposited onto a molten metal bath and controllably cooled to form a float glass ribbon. Examples of float glass processes are disclosed in U.S. Patent Nos. 4,466,562 and 4,671,155 .
  • the first and second plies 12, 18 can each be, for example, clear float glass or can be tinted or colored glass or one ply 12, 18 can be clear glass and the other ply 12, 18 colored glass.
  • examples of glass suitable for the first ply 12 and/or second ply 18 are described in U.S. Patent Nos. 4,746,347 ; 4,792,536 ; 5,030,593 ; 5,030,594 ; 5,240,886 ; 5,385,872 ; and 5,393,593 .
  • the first and second plies 12, 18 can be of any desired dimensions, e.g., length, width, shape, or thickness.
  • the first and second plies can each be 1 mm to 10 mm thick, such as 1 mm to 8 mm thick, such as 2 mm to 8 mm, such as 3 mm to 7 mm, such as 5 mm to 7 mm, such as 6 mm thick.
  • Non-limiting examples of glass that can be used for the practice of the invention include clear glass, Starphire®, Solargreen®, Solextra®, GL-20®, GL-35TM, Solarbronze®, Solargray® glass, Pacifica® glass, SolarBlue® glass, and Optiblue® glass, all commercially available from PPG Industries Inc. of Pittsburgh, Pennsylvania.
  • the solar control coating 30 of the invention is deposited over at least a portion of at least one major surface of one of the glass plies 12, 18. In the example shown in Fig. 1 , the coating 30 is formed over at least a portion of the inner surface 16 of the outboard glass ply 12.
  • the term "solar control coating” refers to a coating comprised of one or more layers or films that affect the solar properties of the coated article, such as, but not limited to, the amount of solar radiation, for example, visible, infrared, or ultraviolet radiation, reflected from, absorbed by, or passing through the coated article; shading coefficient; emissivity, etc.
  • the solar control coating 30 can block, absorb, or filter selected portions of the solar spectrum, such as, but not limited to, the IR, UV, and/or visible spectrums.
  • the solar control coating 30 can be deposited by any conventional method, such as, but not limited to, conventional chemical vapor deposition (CVD) and/or physical vapor deposition (PVD) methods.
  • CVD processes include spray pyrolysis.
  • PVD processes include electron beam evaporation and vacuum sputtering (such as magnetron sputter vapor deposition (MSVD)).
  • Other coating methods could also be used, such as, but not limited to, sol-gel deposition.
  • the coating 30 can be deposited by MSVD. Examples of MSVD coating devices and methods will be well understood by one of ordinary skill in the art and are described, for example, in U.S. Patent Nos. 4,379,040 ; 4,861,669 ; 4,898,789 ; 4,898,790 ; 4,900,633 ; 4,920,006 ; 4,938,857 ; 5,328,768 ; and 5,492,750 .
  • This exemplary coating 230 includes a base layer or first dielectric layer 240 deposited over at least a portion of a major surface of a substrate (e.g., the No. 2 surface 16 of the first ply 12).
  • the first dielectric layer 240 can be a single layer or can comprise more than one film of antireflective materials and/or dielectric materials, such as, but not limited to, metal oxides, oxides of metal alloys, nitrides, oxynitrides, or mixtures thereof.
  • the first dielectric layer 240 can be transparent to visible light.
  • suitable metal oxides for the first dielectric layer 240 include oxides of titanium, hafnium, zirconium, niobium, zinc, bismuth, lead, indium, tin, and mixtures thereof. These metal oxides can have small amounts of other materials, such as manganese in bismuth oxide, tin in indium oxide, etc. Additionally, oxides of metal alloys or metal mixtures can be used, such as oxides containing zinc and tin (e.g., zinc stannate, defined below), oxides of indium-tin alloys, silicon nitrides, silicon aluminum nitrides, or aluminum nitrides.
  • the first dielectric layer 240 can be a substantially single phase film, such as a metal alloy oxide film, e.g., zinc stannate, or can be a mixture of phases composed of zinc and tin oxides or can be composed of a plurality of films.
  • a metal alloy oxide film e.g., zinc stannate
  • the first dielectric layer 240 (whether a single film or multiple film layer) can have a thickness in the range of 100 ⁇ to 600 ⁇ , such as 200 ⁇ to 500 ⁇ , such as 250 ⁇ to 350 ⁇ , such as 250 ⁇ to 310 ⁇ , such as 280 ⁇ to 310 ⁇ , such as 290 ⁇ to 300 ⁇ .
  • the first dielectric layer 240 can comprise a multi-film structure having a first film 242, e.g., a metal alloy oxide film, deposited over at least a portion of a substrate (such as the inner major surface 16 of the first ply 12) and a second film 244, e.g., a metal oxide or oxide mixture film, deposited over the first metal alloy oxide film 242.
  • the first film 242 can be zinc stannate.
  • the first film 242 can be zinc stannate and the second film 244 can be zinc oxide (for example, 90 wt.% zinc oxide and 10 wt.% tin oxide).
  • the first film 242 can comprise zinc stannate having a thickness in the range of 50 ⁇ to 600 ⁇ , such as 50 ⁇ to 500 ⁇ , such as 75 ⁇ to 350 ⁇ , such as 100 ⁇ to 250 ⁇ , such as 150 ⁇ to 250 ⁇ , such as 200 ⁇ to 250 ⁇ , such as 200 ⁇ to 240 ⁇ .
  • the second film 244 can comprise zinc oxide having a thickness in the range of 50 ⁇ to 200 ⁇ , such as 50 ⁇ to 175 ⁇ , such as 50 ⁇ to 150 ⁇ , such as 50 ⁇ to 100 ⁇ .
  • a first heat and/or radiation reflective metallic layer 246 is deposited over the first dielectric layer 240.
  • the first reflective layer 246 can include a reflective metal, such as, but not limited to, metallic gold, copper, palladium, silver, or mixtures, alloys, or combinations thereof.
  • the first reflective layer 246 comprises a metallic silver layer having a thickness in the range of 25 ⁇ to 300 ⁇ , e.g., 50 ⁇ to 300 ⁇ , e.g., 50 ⁇ to 250 ⁇ , e.g., 50 ⁇ to 200 ⁇ , such as 70 ⁇ to 200 ⁇ , such as 100 ⁇ to 200 ⁇ , such as 140 ⁇ to 180 ⁇ .
  • a first primer layer 248 is located over the first reflective layer 246.
  • the first primer layer 248 can be a single film or a multiple film layer.
  • the first primer layer 248 can include an oxygen-capturing material that can be sacrificial during the deposition process to prevent degradation or oxidation of the first reflective layer 246 during the sputtering process or subsequent heating processes.
  • the first primer layer 248 can also absorb at least a portion of electromagnetic radiation, such as visible light, passing through the coating 230. Examples of materials useful for the first primer layer 248 include titanium, Inconel, Stellite®, and mixtures thereof.
  • the first primer layer 248 can have a thickness in the range of 5 ⁇ to 50 ⁇ , e.g., 10 ⁇ to 40 ⁇ , e.g., 15 ⁇ to 30 ⁇ , e.g., 16 ⁇ to 30 ⁇ .
  • a second dielectric layer 250 is located over the first reflective layer 246 (e.g., over the first primer layer 248).
  • the second dielectric layer 250 can comprise one or more metal oxide or metal alloy oxide-containing films, such as those described above with respect to the first dielectric layer 240.
  • the second dielectric layer 250 can include a first metal oxide film 252, e.g., a zinc oxide film, deposited over the first primer film 248 and a second metal alloy oxide film 254, e.g., a zinc stannate (Zn 2 SnO 4 ) film, deposited over the first zinc oxide film 252.
  • An optional third metal oxide film 256 e.g., another zinc oxide layer, can be deposited over the zinc stannate layer.
  • the second dielectric layer 250 can have a total thickness (e.g., the combined thicknesses of the layers) in the range of 50 ⁇ to 1000 ⁇ , e.g., 50 ⁇ to 500 ⁇ , e.g., 100 ⁇ to 370 ⁇ , e.g., 100 ⁇ to 300 ⁇ , e.g., 100 ⁇ to 250 ⁇ , e.g., 200 ⁇ to 230 ⁇ .
  • a total thickness e.g., the combined thicknesses of the layers in the range of 50 ⁇ to 1000 ⁇ , e.g., 50 ⁇ to 500 ⁇ , e.g., 100 ⁇ to 370 ⁇ , e.g., 100 ⁇ to 300 ⁇ , e.g., 100 ⁇ to 250 ⁇ , e.g., 200 ⁇ to 230 ⁇ .
  • the zinc oxide film 252 (and optional third zinc oxide film 256, if present) can have a thickness in the range of 10 ⁇ to 200 ⁇ , e.g., 50 ⁇ to 200 ⁇ , e.g., 60 ⁇ to 150 ⁇ , e.g., 75 ⁇ to 85 ⁇ .
  • the metal alloy oxide layer (zinc stannate) 254 can have a thickness in the range of 50 ⁇ to 800 ⁇ , e.g., 50 ⁇ to 500 ⁇ , e.g., 100 ⁇ to 200 ⁇ , e.g., 155 ⁇ to 200 ⁇ .
  • An absorbing layer 257 is located over the second dielectric layer 250 (e.g., over the third zinc oxide film 256, if present, or over the zinc stannate film 254 if not).
  • the absorbing layer 257 is a multilayer structure having a first absorbing layer 259, a metallic layer 261, and a second absorbing layer 263.
  • the first and second absorbing layers 259, 263 can be the same or different materials.
  • Material suitable for the absorbing layers includes metal or silicon oxide or nitrides.
  • the first and second absorbing layers 259, 265 can be silicon nitride.
  • the first absorbing layer 259 can have a thickness in the range of 10 ⁇ to 200 ⁇ , e.g., 50 ⁇ to 200 ⁇ , e.g., 60 ⁇ to 150 ⁇ , e.g., 80 ⁇ to 90 ⁇ .
  • the second absorbing layer 263 can also be silicon nitride and can have a thickness in the range of 10 ⁇ to 200 ⁇ , e.g., 50 ⁇ to 200 ⁇ , e.g., 60 ⁇ to 150 ⁇ , e.g., 75 ⁇ to 100 ⁇ .
  • the metallic layer 261 is a subcritical thickness layer.
  • the metallic material such as, but not limited to, metallic gold, copper, palladium, aluminum, silver, or mixtures, alloys, or combinations thereof, is applied at a subcritical thickness such that isolated regions or islands of the material are formed rather than a continuous layer of the material.
  • the critical thickness is less than 50 ⁇ , such as less than 40 ⁇ , such as less than 30 ⁇ , such as less than 25 ⁇ .
  • the transition between a continuous layer and a subcritical layer occurs in the range of 25 ⁇ to 50 ⁇ . It is estimated that copper, gold, and palladium would exhibit similar subcritical behavior in this range.
  • the subcritical metallic layer 261 absorbs electromagnetic radiation according to the Plasmon Resonance Theory. This absorption depends at least partly on the boundary conditions at the interface of the metallic islands.
  • the subcritical metallic layer 58 is not an infrared reflecting layer, like the first metallic layer 240.
  • the subcritical layer 261 is not a continuous layer. It is estimated that for silver, the metallic islands or balls of silver metal deposited below the subcritical thickness can have a height of about 2 nm to 7 nm, such as 5 nm to 7 nm. It is estimated that if such subcritical silver layer could be spread out uniformly, it would have a thickness of about 1.1 nm. It is estimated that optically, such discontinuous metal layer behaves as an effective layer thickness of 2.6 nm.
  • the metallic layer 261 is a cobalt-chromium alloy (such as Stellite®) and has a thickness in the range of 1 ⁇ to 50 ⁇ , e.g., 10 ⁇ to 40 ⁇ , e.g., 10 ⁇ to 35 ⁇ , e.g., 10 ⁇ to 30 ⁇ , e.g., 15 ⁇ to 30 ⁇ , e.g., 20 ⁇ to 30 ⁇ , e.g., 25 ⁇ to 30 ⁇ .
  • a cobalt-chromium alloy such as Stellite®
  • a third dielectric layer 262 is deposited over the absorbing layer 257.
  • the third dielectric layer 262 can also include one or more metal oxide or metal alloy oxide-containing layers, such as discussed above with respect to the first and second dielectric layers 240, 250.
  • the third dielectric layer 262 is a multi-film layer similar to the second dielectric layer 250.
  • the third dielectric layer 262 can include an optional first metal oxide layer 264, e.g., a zinc oxide layer, a second metal alloy oxide-containing layer 266, e.g., a zinc stannate layer deposited over the zinc oxide layer 264 (if present), and an optional third metal oxide layer 268, e.g., another zinc oxide layer, deposited over the zinc stannate (second) layer 266.
  • the first zinc oxide layer 264 (if present) and the third zinc oxide layer 268 can each have a thickness in the range of 50 ⁇ to 200 ⁇ , such as 75 ⁇ to 150 ⁇ , such as 80 ⁇ to 150 ⁇ , such as 95 ⁇ to 105 ⁇ .
  • the metal alloy oxide layer (second) 266 can have a thickness in the range of 100 ⁇ to 800 ⁇ , e.g., 200 ⁇ to 700 ⁇ , e.g., 300 ⁇ to 600 ⁇ , e.g., 380 ⁇ to 500 ⁇ , e.g., 420 ⁇ to 450 ⁇ .
  • the total thickness of the third dielectric layer 262 (e.g., the combined thicknesses of the zinc oxide and zinc stannate layers) is in the range of 200 ⁇ to 1000 ⁇ , e.g., 400 ⁇ to 900 ⁇ , e.g., 500 ⁇ to 900 ⁇ , e.g., 500 ⁇ to 600 ⁇ , e.g., 525 ⁇ to 550 ⁇ .
  • a third heat and/or radiation reflective metallic layer 270 is deposited over the third dielectric layer 262.
  • the third reflective layer 270 can be of any of the materials discussed above with respect to the first and second reflective layers.
  • the third reflective layer 270 includes silver and has a thickness in the range of 25 ⁇ to 300 ⁇ , e.g., 50 ⁇ to 300 ⁇ , e.g., 50 ⁇ to 200 ⁇ , such as 70 ⁇ to 150 ⁇ , such as 100 ⁇ to 150 ⁇ , such as 128 ⁇ to 150 ⁇ .
  • a third primer layer 272 is located over the third reflective layer 270.
  • the third primer layer 272 can be as described above with respect to the first or second primer layers.
  • the third primer layer is titanium and has a thickness in the range of 5 ⁇ to 50 ⁇ , e.g., 10 ⁇ to 30 ⁇ , e.g., 17 ⁇ to 30 ⁇ .
  • a fourth dielectric layer 274 is located over the third reflective layer (e.g., over the third primer layer 272).
  • the fourth dielectric layer 274 can be comprised of one or more metal oxide or metal alloy oxide-containing layers, such as those discussed above with respect to the first, second, or third dielectric layers 240, 250, 262.
  • the fourth dielectric layer 274 is a multi-film layer having a first metal oxide layer 276, e.g., a zinc oxide layer, deposited over the third primer film 272, and a second metal alloy oxide layer 278, e.g., a zinc stannate layer, deposited over the zinc oxide layer 276.
  • the zinc oxide layer 276 can have a thickness in the range of 25 ⁇ to 200 ⁇ , such as 50 ⁇ to 150 ⁇ , such as 60 ⁇ to 100 ⁇ , such as 60 ⁇ to 70 ⁇ .
  • the zinc stannate layer 78 can have a thickness in the range of 25 ⁇ to 500 ⁇ , e.g., 50 ⁇ to 500 ⁇ , e.g., 100 ⁇ to 400 ⁇ , e.g., 150 ⁇ to 300 ⁇ , e.g., 150 ⁇ to 200 ⁇ , e.g., 180 ⁇ to 190 ⁇ .
  • the total thickness of the fourth dielectric layer 274 (e.g., the combined thickness of the zinc oxide and zinc stannate layers) is in the range of 100 ⁇ to 800 ⁇ , e.g., 200 ⁇ to 600 ⁇ , e.g., 250 ⁇ to 400 ⁇ , e.g., 250 ⁇ to 270 ⁇ .
  • An overcoat 280 is located over the fourth dielectric layer 274.
  • the overcoat 280 can help protect the underlying coating layers from mechanical and chemical attack.
  • the overcoat 280 can be, for example, a metal oxide or metal nitride layer.
  • the overcoat 280 can be titania having a thickness in the range of 10 ⁇ to 100 ⁇ , such as 20 ⁇ to 80 ⁇ , such as 30 ⁇ to 50 ⁇ , such as 30 ⁇ to 40 ⁇ .
  • the subcritical metal e.g. silver
  • another layer such as a metal oxide or metal layer can be applied over the subcritical silver layer to essentially encapsulate and protect the metal, e.g. silver, islands.
  • a nanocomposite layer can be deposited with a nanocrystalline metallic phase embedded or incorporated within a dielectric matrix phase.
  • Fig. 3 shows a nanocomposite layer 382 having a first material 384 with metallic nanoparticles 386 incorporated into the first material 382 deposited on a substrate 388.
  • This nanocomposite layer 382 could take the place of one or more metallic layers in a solar control coating according to the present invention, for example, such as any of the coatings described above.
  • a nanocomposite layer 382 could be provided by conventional reactive sputtering using a target having a first material and at least one second material.
  • the first material can be a material that has a relatively stronger tendency to nitride or oxidize than the second material. These materials could be present either as alloys or as a composite target.
  • the first material could be Cr, Al, Ti, or Si.
  • the second material could be a noble metal, such as Ag, Cu, or Au or a transition metal including Fe, Ni, or Co.
  • the first material oxidizes and forms a dielectric matrix phase and the second material is contained within the phase, such as in the form of metal nanoparticles.
  • the nanocomposite layer 382 can be adjusted by appropriate selection of the reactive gas, sputtering voltage, etc., to form a nanocomposite layer of a desired thickness.
  • This nanocomposite layer 382 having the metallic particles 386 embedded within the first material 384 can better withstand the high temperatures associated with heat treating or tempering than coatings with continuous metallic films.
  • One way to do this would be by the use of integrating a semiconductor material into a solar control coating that has a band gap edge in the visible region of the electromagnetic spectrum.
  • a semiconductor material into a solar control coating that has a band gap edge in the visible region of the electromagnetic spectrum.
  • shorter wave length radiation is absorbed by the semiconductor material while longer wavelength energy is transmitted through the material. That is, the material is transparent to radiation above the edge of the band gap.
  • the absorption edge can be placed near the long-wavelength side of the visible spectrum. In this way, the optical transmission can be reduced without absorbing near or far infrared radiation, minimizing unnecessary heating of the glass into absorption.
  • This semiconductor material can be placed within a conventional solar control coating, such as between two silver layers, above a silver layer, below a silver layer, or anywhere else within the stack.
  • Rf refers to the film side reflectance
  • Rg refers to the glass side reflectance
  • T refers to the transmittance through the article
  • Rg60 refers to the glass side reflectance at a 60 degree angle
  • Rx refers to the exterior reflectance of a standard IGU from the No. 1 surface
  • Rint refers to the reflectance of the IGU from the inside (No. 4) surface
  • VLT refers to the visible light transmittance
  • SHGC refers to the solar heat gain coefficient.
  • a “standard IGU” has an outer ply of 6 mm thick glass, an inner ply of 6 mm glass, a 0.5 inch (1.27 cm) gap filled with air, with the coating on the No. 2 surface.
  • S.C means "subcritical" thickness (that is, the layer was not a continuous layer but was deposited to form discontinuous coating regions.)
  • heat treated means that the coated substrate was heated in a box furnace to a temperature of 1,185°F to simulate tempering and then air cooled to room temperature before the optical characteristics were measured.
  • the color coordinates a*, b*, and L* are those of the conventional CIE (1931) and CIELAB systems that will be understood by one of ordinary skill in the art.
  • the subcritical layer can be modeled as two idealized layers. These idealized layers have uniform optical properties (i.e., index of refraction (n) and extinction co-efficient (k)) through their thickness, as do the other layers in the stack.
  • n index of refraction
  • k extinction co-efficient
  • the thicknesses referred to in the examples are the thicknesses of these idealized layers and are meaningful in the context of calculating the optical response of a given coating stack containing these layers.
  • the thickness values associated with the "subcritical" layers in the following Examples are "effective thickness" calculated based on a reference coating speed that is slower than the actual coating speed of the commercial coater. For example, a silver layer is applied onto a substrate at the same coating rate as a commercial coater but at a reduced line speed (reference coating speed) compared to the commercial coater. The thickness of the coating deposited at the reference coating speed is measured and then the "effective thickness" for a coating deposited at the same coating rate but at the faster line speed of the commercial coater is extrapolated.
  • the "effective thickness" of the silver layer at the same coating rate but at the commercial coater line speed is extrapolated to be 25 ⁇ (i.e., one tenth the thickness).
  • the silver layer at this effective thickness would not be a continuous layer but rather would be a discontinuous layer having discontinuous regions of silver material.
  • a coating was deposited by a conventional MSVD coater (commercially available from Applied Materials) on a 6 mm piece of clear glass.
  • the coated glass had the following structure: titania 40 ⁇ zinc stannate 190 ⁇ zinc oxide (90/10) 80 ⁇ titanium 30 ⁇ silver 150 ⁇ zinc oxide 120 ⁇ zinc stannate 450 ⁇ zinc oxide 120 ⁇ Inconel 22 ⁇ S.C. silver 25 ⁇ zinc stannate 110 ⁇ zinc oxide 70 ⁇ titanium 30 ⁇ silver 180 ⁇ zinc oxide 110 ⁇ zinc stannate 200 ⁇ clear glass 6 mm
  • This coated glass was heat treated as described above and had the optical characteristics shown in Table 1 below.
  • the article was incorporated into a standard IGU as the outer ply (the inner ply was uncoated 6 mm clear glass) and had the optical characteristics set forth in Table 2 below.
  • a coating was deposited by a conventional Airco MSVD coater on a 6 mm piece of Starphire® glass.
  • the coated glass had the following structure: titania 40 ⁇ zinc stannate 170 ⁇ zinc oxide (90/10) 80 ⁇ titanium 20 ⁇ silver 150 ⁇ zinc oxide 120 ⁇ zinc stannate 480 ⁇ zinc oxide 120 ⁇ Inconel 22 ⁇ S.C. silver 25 ⁇ zinc stannate 110 ⁇ zinc oxide 70 ⁇ titanium 20 ⁇ silver 180 ⁇ zinc oxide 110 ⁇ zinc stannate 220 ⁇ Starphire® glass 6 mm
  • This coated glass was heat treated as described above and had the optical characteristics shown in Table 1 below.
  • the article was incorporated into a standard IGU as the outer ply (the inner ply was uncoated 6 mm Starphire® glass) and had the optical characteristics set forth in Table 2 below.
  • a coating was deposited by a conventional Airco MSVD coater on a 6 mm piece of Optiblue® glass.
  • the coated glass had the following structure: titania 40 ⁇ zinc stannate 170 ⁇ zinc oxide (90/10) 80 ⁇ titanium 20 ⁇ silver 150 ⁇ zinc oxide 120 ⁇ zinc stannate 480 ⁇ zinc oxide 120 ⁇ Inconel 22 ⁇ S.C. silver 25 ⁇ zinc stannate 110 ⁇ zinc oxide 70 ⁇ titanium 20 ⁇ silver 180 ⁇ zinc oxide 110 ⁇ zinc stannate 220 ⁇ Optiblue® glass 6 mm
  • This coated glass was heat treated as described above and had the optical characteristics shown in Table 1 below.
  • the article was incorporated into a standard IGU as the outer ply (the inner ply was uncoated 6 mm Starphire® glass) and had the optical characteristics set forth in Table 2 below.
  • a coating was deposited by a conventional Airco MSVD coater on a 6 mm piece of clear glass.
  • the coated glass had the following structure: titania 40 ⁇ zinc stannate 200 ⁇ zinc oxide (90/10) 70 ⁇ titanium 30 ⁇ silver 170 ⁇ zinc oxide 100 ⁇ zinc stannate 560 ⁇ zinc oxide 100 ⁇ titanium 30 ⁇ S.C. silver 25 ⁇ Zinc oxide 50 ⁇ zinc stannate 270 ⁇ zinc oxide 50 ⁇ titanium 30 ⁇ silver 120 ⁇ zinc oxide 70 ⁇ zinc stannate 140 ⁇ clear glass 6 mm
  • This coated glass was heat treated as described above and had the optical characteristics shown in Table 1 below.
  • the article was incorporated into a standard IGU as the outer ply (the inner ply was uncoated 6 mm clear glass) and had the optical characteristics set forth in Table 2 below.
  • a coating was deposited by a conventional Airco MSVD coater on a 6 mm piece of clear glass.
  • the coated glass had the following structure: titania 40 ⁇ zinc stannate 170 ⁇ zinc oxide (90/10) 80 ⁇ titanium 30 ⁇ silver 137 ⁇ zinc oxide 95 ⁇ zinc stannate 380 ⁇ zinc oxide 95 ⁇ Inconel 15 ⁇ S.C. silver 30 ⁇ zinc stannate 235 ⁇ zinc oxide 85 ⁇ titanium 30 ⁇ silver 125 ⁇ zinc oxide 100 ⁇ zinc stannate 200 ⁇ clear glass 6 mm
  • This coated glass was heat treated as described above and had the optical characteristics shown in Table 1 below.
  • the article was incorporated into a standard IGU as the outer ply (the inner ply was uncoated 6 mm clear glass) and had the optical characteristics set forth in Table 2 below.
  • a coating was deposited by a conventional Airco MSVD coater on a 6 mm piece of clear glass.
  • the coated glass had the following structure: titania 40 ⁇ zinc stannate 320 ⁇ zinc oxide (90/10) 150 ⁇ titanium 15 ⁇ Inconel 15 ⁇ silver 170 ⁇ zinc oxide 75 ⁇ zinc stannate 500 ⁇ zinc oxide 75 ⁇ titanium 15 ⁇ Inconel 5 ⁇ silver 73 ⁇ zinc oxide 85 ⁇ zinc stannate 355 ⁇ clear glass 6 mm
  • This coated glass was not heat treated and had the optical characteristics shown in Table 1 below.
  • the article was incorporated into a standard IGU as the outer ply (the inner ply was uncoated 6 mm clear glass) and had the optical characteristics set forth in Table 2 below.
  • a coating was deposited by a conventional Airco MSVD coater on a 6 mm piece of clear glass.
  • the coated glass had the following structure: titania 40 ⁇ zinc stannate 190 ⁇ zinc oxide (90/10) 60 ⁇ titanium 17 ⁇ silver 128 ⁇ zinc oxide 105 ⁇ zinc stannate 420 ⁇ zinc oxide 120 ⁇ silicon nitride 100 ⁇ Stellite® 30 ⁇ silicon nitride 80 ⁇ zinc stannate 155 ⁇ zinc oxide 75 ⁇ titanium 16 ⁇ silver 140 ⁇ zinc oxide 50 ⁇ zinc stannate 240 ⁇ clear glass 6 mm
  • This coated glass was not heat treated and the had optical characteristics shown in Table 1 below.
  • the article was incorporated into a standard IGU as the outer ply (the inner ply was uncoated 6 mm clear glass) and had the optical characteristics set forth in Table 2 below.
  • a coating was deposited by a conventional Airco MSVD coater on a 6 mm piece of clear glass.
  • the coated glass had the following structure: titania 40 ⁇ zinc stannate 180 ⁇ zinc oxide (90/10) 70 ⁇ titanium 30 ⁇ silver 128 ⁇ zinc oxide 105 ⁇ zinc stannate 420 ⁇ zinc oxide 120 ⁇ silicon nitride 100 ⁇ Stellite® 30 ⁇ silicon nitride 80 ⁇ zinc stannate 155 ⁇ zinc oxide 75 ⁇ titanium 30 ⁇ silver 140 ⁇ zinc oxide 50 ⁇ zinc stannate 240 ⁇ clear glass 6 mm
  • This coated glass was heat treated as described above and had the optical characteristics shown in Table 1 below.
  • the article was incorporated into a standard IGU as the outer ply (the inner ply was uncoated 6 mm clear glass) and had the optical characteristics set forth in Table 2 below.
  • a coating was deposited by a conventional Airco MSVD coater on a 6 mm piece of clear glass.
  • the coated glass had the following structure: titania 43 ⁇ zinc stannate 196 ⁇ zinc oxide (90/10) 81 ⁇ titanium 33 ⁇ silver 151 ⁇ zinc oxide 120 ⁇ zinc stannate 448 ⁇ zinc oxide 120 ⁇ Inconel 22 ⁇ S.C. silver 26 ⁇ zinc stannate 116 ⁇ zinc oxide 70 ⁇ titanium 35 ⁇ silver 182 ⁇ zinc oxide 110 ⁇ zinc stannate 198 ⁇ clear glass 6 mm TABLE 1 Example No.

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Claims (14)

  1. Ein beschichteter Gegenstand umfassend:
    ein Substrat (12); und
    eine Beschichtung (230) über wenigstens einem Teil des Substrats (12), wobei die Beschichtung (230) umfasst:
    eine erste dielektrische Schicht (240) aufgebracht über wenigstens einem Teil des Substrates (12);
    eine erste wärme- und/oder strahlungsreflektierende metallische Schicht (246) aufgebracht über der ersten dielektrischen Schicht (240);
    eine erste Primerschicht (248) angeordnet über der ersten wärme- und/oder strahlungsreflektierenden metallischen Schicht (246),
    eine zweite dielektrische Schicht (250) angeordnet über der ersten Primerschicht (248);
    eine absorbierende Mehrschichtstruktur (257) angeordnet über der zweiten dielektrischen Schicht (250), wobei die absorbierende Mehrschichtstruktur (257) eine erste absorbierende Schicht (259), eine metallische Schicht aufweisend eine subkritische Dicke (261), sodass das Beschichtungsmaterial isolierte, nicht-verbundene Regionen des Beschichtungsmaterials bildet, und eine zweite absorbierende Schicht (263) umfasst;
    eine dritte dielektrische Schicht (262) aufgebracht über der absorbierenden Schicht (263);
    eine dritte wärme- und/oder strahlungsreflektierende metallische Schicht (270) aufgebracht über der dritten dielektrischen Schicht (262),
    eine dritte Primerschicht (272) angeordnet über der dritten wärme- und/oder strahlungsreflektierenden metallischen Schicht (270);
    eine vierte dielektrische Schicht (274) angeordnet über der dritten Primerschicht (272); und
    einen schützenden Überzug (280) angeordnet über der vierten dielektrischen Schicht (274).
  2. Der Gegenstand gemäß Anspruch 1, wobei die metallische Schicht (261) der absorbierenden Mehrschichtstruktur (257) eine Cobalt-Chrom-Legierungsschicht aufweisend eine Dicke im Bereich von 1 Å bis 50 Å ist.
  3. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei die erste absorbierende Schicht (259) und/oder die zweite absorbierende Schicht (263) Siliziumnitrid umfasst.
  4. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei die erste Primerschicht (248) und/oder die dritte Primerschicht (272) Titan umfasst.
  5. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei die erste wärme- und/oder strahlungsreflektierende metallische Schicht (246) und/oder die dritte wärme- und/oder strahlungsreflektierende metallische Schicht (270) metallisches Gold, Kupfer, Palladium, Aluminium, Silber oder Mischungen, Legierungen oder Kombinationen derselben umfasst.
  6. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei die erste wärme- und/oder strahlungsreflektierende metallische Schicht (246) und/oder die dritte wärme- und/oder strahlungsreflektierende metallische Schicht (270) metallisches Silber umfasst.
  7. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei das Substrat (12) ein Glassubstrat ist.
  8. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei der schützende Überzug (280) eine Metalloxid- oder Metallnitridschicht ist, wobei der schützende Überzug bevorzugt aus Titanoxid hergestellt ist.
  9. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei eine oder mehrere von der ersten dielektrischen Schicht (240), der zweiten dielektrischen Schicht (250), der dritten dielektrischen Schicht (262) und der vierten dielektrischen Schicht (274) eine oder mehrere Metalloxid- oder Metalllegierungsoxid-enthaltende Schichten umfasst.
  10. Der Gegenstand gemäß Anspruch 9, wobei das Metalloxid aus Oxiden von Titan, Hafnium, Zirkonium, Niob, Zink, Bismut, Blei, Indium, Zinn und Mischungen derselben ausgewählt ist.
  11. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei die erste dielektrische Schicht eine Metalloxidschicht (214), vorzugsweise eine Zinkoxidschicht, aufgebracht über einer Metalllegierungsoxidschicht (242), vorzugsweise einer Zinkstannatschicht, umfasst.
  12. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei die zweite dielektrische Schicht (250) eine Metalllegierungsoxidschicht (254), vorzugsweise eine Zinkstannatschicht, aufgebracht über einer Metalloxidschicht (252), vorzugsweise einer Zinkoxidschicht, umfasst.
  13. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei die dritte dielektrische Schicht (262) eine Metalllegierungsoxidschicht (266), vorzugsweise eine Zinkstannatschicht, aufgebracht über einer Metalloxidschicht (264), vorzugsweise einer Zinkoxidschicht, und wahlweise eine weitere Metalloxidschicht (268), vorzugsweise eine Zinkoxidschicht, aufgebracht über der Metalllegierungsoxidschicht (266) umfasst.
  14. Der Gegenstand gemäß irgendeinem der vorstehenden Ansprüche, wobei die vierte dielektrische Schicht (274) eine Metalllegierungsoxidschicht (278), vorzugsweise eine Zinkstannatschicht, aufgebracht über einer Metalloxidschicht (276), vorzugsweise einer Zinkoxidschicht, umfasst.
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US20140272453A1 (en) * 2013-03-12 2014-09-18 Ppg Industries Ohio, Inc. Solar Control Coatings Providing Increased Absorption Or Tint
US10654747B2 (en) * 2010-03-29 2020-05-19 Vitro Flat Glass Llc Solar control coatings with subcritical copper
FR2988387B1 (fr) * 2012-03-21 2017-06-16 Saint Gobain Vitrage de controle solaire
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US20220144697A1 (en) 2022-05-12
US9932267B2 (en) 2018-04-03
US11993536B2 (en) 2024-05-28
US11267752B2 (en) 2022-03-08
CN102811966A (zh) 2012-12-05
JP5705963B2 (ja) 2015-04-22
BR112012024473A2 (pt) 2016-05-31
HUE052235T2 (hu) 2021-04-28
US20110236715A1 (en) 2011-09-29
CO6571862A2 (es) 2012-11-30
RU2012145869A (ru) 2014-05-10
AU2011235302B2 (en) 2014-04-03
RU2535555C2 (ru) 2014-12-20
AU2011235302A1 (en) 2012-08-23
KR101464847B1 (ko) 2014-11-25
BR112012024473B1 (pt) 2020-01-21
US20190276352A1 (en) 2019-09-12

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